HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phosphorus oxychloride → 2,9-Di-tert-butyl-6-chlorophenanthridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | Phosphorus pentachloride | HCID 24819 | — |
| Reactant | 2,9-Di-t-butylphenanthridinone | HCID 66813594 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2,9-Di-tert-butyl-6-chlorophenanthridine | HCID 57437659 | 98% |
Reaction Steps
The above 2,9-di-t-butylphenanthridinone (3.0 g, 9.7 mmole) was added to a reaction flask containing phosphorus pentachloride (3.0 g, 14.6 mmole) and 50 mL of phosphoryl chloride. The reaction mixture was refluxed overnight, cooled to room temperature and diluted with toluene. The excess phosphoryl chloride and toluene were removed by a rotary evaporator. The residue was dissolved into ethyl acetate and washed with distilled water followed by brine. The solvent layer was dried over magnesium sulfate, filtered and concentrated to give the desired 2,9-di-tert-butyl-6-chlorophenanthridine (3.0 grams, 98%) as an off white solid. The product was confirmed by GC Mass Spec and not purified further but used directly in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08691988B2 |
| Source dataset | uspto-grants-2014_04 |
| ORD ID | ord-4e98cf852ce949dbbc5ba47b9a1c1078 |
| Source note | uspto-grants-2014_04 |